![Health / Center for Devices and Radiological Health / Premarket approval / Unique Device Identification / Medical device / Federal Food / Drug / and Cosmetic Act / Title 21 of the Code of Federal Regulations / Adverse event / Investigational Device Exemption / Food and Drug Administration / Medicine / Technology Health / Center for Devices and Radiological Health / Premarket approval / Unique Device Identification / Medical device / Federal Food / Drug / and Cosmetic Act / Title 21 of the Code of Federal Regulations / Adverse event / Investigational Device Exemption / Food and Drug Administration / Medicine / Technology](https://www.pdfsearch.io/img/c53bd145d91b0465543c1febc4eb5a31.jpg) Date: 2015-03-03 15:35:30Health Center for Devices and Radiological Health Premarket approval Unique Device Identification Medical device Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Adverse event Investigational Device Exemption Food and Drug Administration Medicine Technology | | DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration[removed]New Hampshire AvenueAdd to Reading ListSource URL: www.accessdata.fda.govDownload Document from Source Website File Size: 71,43 KBShare Document on Facebook
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